{
    "disease_id": "DOID:0110192", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "FGD4 Charcot-Marie-Tooth disease type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "Charcot-Marie-Tooth disease, autosomal recessive, type 4H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "Charcot-Marie-Tooth disease type 4 caused by mutation in FGD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "autosomal recessive Charcot-Marie-Tooth disease type 4H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "Charcot-Marie-Tooth disease, type 4H; CMT4H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "CMT4H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "Charcot-Marie-Tooth neuropathy, type 4H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "Charcot-Marie-Tooth disease, type 4H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012250", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012250", 
            "name": "Charcot-Marie-Tooth neuropathy type 4H"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110192", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110192", 
            "name": "autosomal recessive Charcot-Marie-Tooth disease type 4H"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110192", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110192", 
            "name": "CMT4H"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110192", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110192", 
            "name": "Charcot-Marie-Tooth neuropathy type 4H"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110192", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110192", 
            "name": "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110192", 
        "description": "A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutations in the gene encoding frabin (FGD4).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110192", 
        "name": "Charcot-Marie-Tooth disease type 4H"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110192#disease-associations", 
            "id": "0110192", 
            "database": "Alliance of Genome Resources"
        }
    ]
}